Poster

P15.2 – Impact of Thermal Treatment on the Mechanical and Structural Properties of Nanocellulose Filaments

Mu-Rong Wang

KTH, Royal Institute of Technology

Co-author(s):
Korneliya Gordeyeva, KTH, Royal Institute of Technology
Daniel Söderberg, KTH, Royal Institute of Technology

The outstanding mechanical properties of cellulose have long motivated us to use it as a sustainable source to improve the mechanical properties of materials. After isolating cellulose from wood pulp and defibrillating it into nanocellulose, the reported mechanical stiffness ranges between 110-150 GPa.[1, 2] Since 2014, a spinning process utilising a flow-focusing microfluidic device that aligns and structures nanofibers into continuous filaments has been developed.[3] This process led to the production of the strongest bio-based filaments, with a reported stiffness of 86 GPa.[4] To provide a basis for upscaling of the spinning process, we have investigated the effect of elevated drying temperatures (60 °C, 105 °C, and 160 °C) on filament mechanical properties, comparing them to filaments dried at ambient conditions (20 °C). We observed a decrease in mechanical performance up to 105 °C, followed by an increase at 160 °C. To understand the underlying structural changes responsible for this trend, we analysed the filaments using Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and Atomic Force Microscopy (AFM) and correlated the findings with the observed mechanical behaviour.

References:[1] T. Saito, R. Kuramae, J. Wohlert, L. A. Berglund, and A. Isogai, “An ultrastrong nanofibrillar biomaterial: the strength of single cellulose nanofibrils revealed via sonication-induced fragmentation,” Biomacromolecules, vol. 14, no. 1, pp. 248-253, 2013. [2] A. Idström, H. Brelid, M. Nydén, and L. Nordstierna, “CP/MAS 13C NMR study of pulp hornification using nanocrystalline cellulose as a model system,” Carbohydrate polymers, vol. 92, no. 1, pp. 881-884, 2013. [3] K. M. O. Håkansson et al., “Hydrodynamic alignment and assembly of nanofibrils resulting in strong cellulose filaments,” Nature Communications, vol. 5, no. 1, 2014, doi: 10.1038/ncomms5018. [4] N. Mittal et al., “Multiscale Control of Nanocellulose Assembly: Transferring Remarkable Nanoscale Fibril Mechanics to Macroscale Fibers,” ACS Nano, vol. 12, no. 7, pp. 6378-6388, 2018, doi: 10.1021/acsnano.8b01084.

Session: 

Time: